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内影像携带抗独特型单克隆抗体。

Internal image-bearing anti-idiotypic monoclonal antibodies.

作者信息

Hinoda Y, Tsujisaki M, Imai K, Yachi A

机构信息

Department of Internal Medicine (Section 1), Sapporo Medical University School of Medicine, Japan.

出版信息

Tumour Biol. 1995;16(1):48-55. doi: 10.1159/000217928.

Abstract

Five anti-idiotypic (Id) monoclonal antibodies (MAbs) (Ab2) were prepared from a BALB/c mouse immunized with anti-carcinoembryonic antigen (CEA) MAb MA208 (Ab1) in a syngeneic system. These anti-Id MAbs appear to recognize unique idiotopes at the combining site of MAb MA208, because they were specifically reactive with MAb MA208 and showed inhibitory activity against the binding of MAb MA208 to CEA. These MAbs were divided into three groups according to the analysis of anti-anti-Id antibodies (Ab3) induced with each anti-Id MAb. Anti-anti-Id MAb M7-625 antiserum (Ab3) reacted with purified CEA in a binding assay and in Western blot analysis, and competed with Ab1 binding to CEA. Furthermore, the binding of anti-Id MAb M7-625 to MAb MA208 was inhibited with CEA, indicating that Ab2 mimics the structure of the epitope in CEA which was recognized with Ab1. These serologic findings suggest that anti-Id MAb M7-625 carries the internal image of the antigen. According to the amino acid sequences of complementarity determining region (CDR) 1, 2 and 3 of the MAb M7-625 variable region, homology of amino acid sequences exists between CDR2 in the H chain (5 amino acids of 10) and domain III of CEA (545-554). Seven anti-Id MAbs were then generated using anti-CEA synthetic peptide MAb P1-356 to analyze further the epitope structure of CEA. These anti-Id MAbs were divided into four groups. Serological analyses as described above suggested that among them, anti-Id MAb M315 had an internal image. We therefore prepared anti-anti-Id MAbs using anti-Id MAb M315. Among them, anti-anti-Id MAb 11B2 reacted directly with CEA and competed with MAb P1-356 in the competition assay. In addition, MAb 11B2 stained both cultured CEA-producing cells and colonic cancer tissues, suggesting that MAb 11B2 is Ab1 like Ab3. These MAbs (Ab1-3) will be of use for the structural analysis of the internal image.

摘要

用抗癌胚抗原(CEA)单克隆抗体MA208(Ab1)在同基因系统中免疫BALB/c小鼠,制备了5种抗独特型(Id)单克隆抗体(MAb)(Ab2)。这些抗Id单克隆抗体似乎在MAb MA208的结合位点识别独特的独特型,因为它们与MAb MA208特异性反应,并对MAb MA208与CEA的结合表现出抑制活性。根据每种抗Id单克隆抗体诱导产生的抗抗Id抗体(Ab3)分析,这些单克隆抗体被分为三组。抗抗Id单克隆抗体M7-625抗血清(Ab3)在结合试验和蛋白质印迹分析中与纯化的CEA反应,并与Ab1结合CEA竞争。此外,CEA抑制抗Id单克隆抗体M7-625与MAb MA208的结合,表明Ab2模拟了CEA中被Ab1识别的表位结构。这些血清学结果表明抗Id单克隆抗体M7-625携带抗原的内影像。根据单克隆抗体M7-625可变区互补决定区(CDR)1、2和3的氨基酸序列,重链中的CDR2(10个中的5个氨基酸)与CEA的结构域III(545-554)之间存在氨基酸序列同源性。然后用抗CEA合成肽单克隆抗体P1-356产生7种抗Id单克隆抗体,以进一步分析CEA的表位结构。这些抗Id单克隆抗体被分为四组。如上所述的血清学分析表明,其中抗Id单克隆抗体M315具有内影像。因此,我们用抗Id单克隆抗体M315制备了抗抗Id单克隆抗体。其中,抗抗Id单克隆抗体11B2直接与CEA反应,并在竞争试验中与单克隆抗体P1-356竞争。此外,单克隆抗体11B2对培养的CEA产生细胞和结肠癌组织均有染色,表明单克隆抗体11B2与Ab3一样是Ab1。这些单克隆抗体(Ab1-3)将用于内影像的结构分析。

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